Kitko Carrie L, Braun Thomas, Couriel Daniel R, Choi Sung W, Connelly James, Hoffmann Sandra, Goldstein Steven, Magenau John, Pawarode Attaphol, Reddy Pavan, Schuler Charles, Yanik Gregory A, Ferrara James L, Levine John E
Blood and Marrow Transplant Program, University of Michigan, Ann Arbor, Michigan; Pediatric Stem Cell Transplant Program, Vanderbilt University, Nashville, Tennessee.
Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan.
Biol Blood Marrow Transplant. 2016 May;22(5):862-8. doi: 10.1016/j.bbmt.2015.11.002. Epub 2015 Nov 6.
Reduced-intensity conditioning (RIC) regimens minimize early toxicity after allogeneic hematopoietic cell transplantation (HCT) by placing greater reliance on establishing a graft-versus-leukemia effect (GVL). Because graft-versus-host disease (GVHD) and GVL are tightly linked, inhibition of T cell populations that cause GVHD may lead to an unintended increased risk of relapse in the RIC setting. Although not completely understood, etanercept and extracorporeal photopheresis (ECP) are thought to ameliorate GVHD without direct T cell inhibition. We hypothesized that adding these 2 agents to a standard GVHD prophylaxis regimen of tacrolimus and mycophenolate mofetil (MMF) would improve survival by reducing GVHD-related mortality without increasing relapse rates. Therefore, we conducted a prospective phase II clinical trial that incorporated tacrolimus, MMF, etanercept, and ECP as GVHD prophylaxis in 48 patients undergoing RIC unrelated donor transplantation. The preferred RIC was fludarabine 160 mg/m(2) + busulfan 6.4 mg/kg to 12.8 mg/kg ± total body irradiation 200 cGy. Etanercept .4 mg/kg (maximum dose, 25 mg) was given subcutaneously twice weekly for 8 weeks after HCT and ECP was given for 12 treatments, starting weekly on day 28 weekly and tapering off by day 180. The median age of the study patients was 60 (range, 18 to 71) years. Donors were 7/8 (n = 14, 29%) or 8/8 (n = 34, 71%) HLA matched. All patients engrafted neutrophils at a median of 12 days. The cumulative incidence of grades II to IV acute GVHD at day 100 was 46%, but it was typically sensitive to initial steroid treatment (84% day 56 complete response/partial response rate). Overall survival at 1 year in this older, frequently mismatched unrelated donor setting was excellent (73%) because of low rates of nonrelapse mortality (21%) and relapse (19%). However, this strategy was not effective at preventing a high incidence of chronic GVHD and late deaths led to a drop in 2-year survival, declining to 56%, reflecting a high incidence of chronic GVHD.
减低强度预处理(RIC)方案通过更多地依赖建立移植物抗白血病效应(GVL),将异基因造血细胞移植(HCT)后的早期毒性降至最低。由于移植物抗宿主病(GVHD)和GVL紧密相关,在RIC情况下,抑制引起GVHD的T细胞群体可能会导致意外的复发风险增加。尽管尚未完全了解,但依那西普和体外光化学疗法(ECP)被认为可改善GVHD而不直接抑制T细胞。我们假设,在他克莫司和霉酚酸酯(MMF)的标准GVHD预防方案中加入这两种药物,将通过降低与GVHD相关的死亡率而不增加复发率来提高生存率。因此,我们进行了一项前瞻性II期临床试验,在48例接受RIC无关供体移植的患者中,将他克莫司、MMF、依那西普和ECP作为GVHD预防措施。首选的RIC方案是氟达拉滨160mg/m² + 白消安6.4mg/kg至12.8mg/kg ± 全身照射200cGy。依那西普0.4mg/kg(最大剂量25mg)在HCT后每周皮下注射两次,共8周,ECP进行12次治疗,从第28天开始每周一次,至第180天逐渐减少。研究患者的中位年龄为60岁(范围18至71岁)。供体与患者的人类白细胞抗原(HLA)配型为7/8(n = 14,29%)或8/8(n = 34,71%)。所有患者中性粒细胞中位植入时间为12天。第100天时II至IV级急性GVHD的累积发生率为46%,但通常对初始类固醇治疗敏感(第56天时完全缓解/部分缓解率为84%)。在这个年龄较大、经常配型不合的无关供体情况下,1年总生存率极佳(73%),这是因为非复发死亡率(21%)和复发率(19%)较低。然而,该策略在预防慢性GVHD的高发生率方面并不有效,晚期死亡导致2年生存率下降至56%,这反映了慢性GVHD的高发生率。